Showing entry for Velopharyngeal Insufficiency
| General Disease Information | |
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| BXGD Id | BXGD002983 |
| Disease Name | Velopharyngeal Insufficiency |
| Disease CUI Id | C0042454 |
| MeSH Codes | C16 C07 C09 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases; Otorhinolaryngologic Diseases |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | HP:0000152 |
| Human Phenotype Ontology Term | Abnormality of head or neck |
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| Disorder Network | disorder-protein-compound-food associations |
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